内容简介
The Third Edition presents all pharmaceutical industry personnel and those in academia with critical updates on the recent advances in granulation technology and changes in FDA regulatory guidelines. Addressing precisely how these recent innovations and revisions affect unit operation of particle generation and granulation, this text assists the reader in selecting the ideal technology for his/her company's particular drug delivery system. This knowledge helps ensure that regulatory guidelines are followed and met in a cost-effective manner. Here are just a few of the new topics discussed in this revised and expanded handbook: ULLIspray drying/LILInanotechnology/LILIbiotechnologically derived drugs/LILInutraceuticals/LILIcontrolled release drugs/LILIparticle engineering/LILIsupercritical fluids/LILIconcepts of design space/LILIprocess optimization/LILIregulation harmonization by global health authorities/LILIprocess controlexpert systems/LILIProcess Analytical Technology (PAT)/LILIregulatory issues in granulation/LI/ULIn addition, all chapters in the Handbook of Pharmaceutical Granulation Technology explore the fundamentals of powder characterization, granulation, and state-of-the-art technologies, modeling, application of expert systems, and manufacturing optimization.
